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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

112 — Class I MDD by BSV Kubiš, s.r.o.

MD Atlas
BSV Kubiš, s.r.o.

EUDAMED last updated this device on Jul 14, 2025

112

B-CZMF000040605112WH

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: BSV Kubiš, s.r.o.
UDI-DI code: D-CZMF000040605112WH
Reference / catalog number: 112

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Manufacturer information

Organization name: BSV Kubiš, s.r.o.
SRN: CZ-MF-000040605
Manufacturer status: Active

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Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-CZMF000040605112WH
Basic UDI-DI: B-CZMF000040605112WH
Reference / catalog number: 112
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: nerez
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 0.7 MU50
28 MU50

EMDN nomenclature code(s)

L0202SUTURE NEEDLES, REUSABLE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.